Associate Director Toxicology
Core
Lead reproductive toxicology activities to support the safe progression of drug candidates through clinical development.
Role type
Associate Director, Toxicology
Builds
Drug safety assessments and regulatory submissions for clinical development
Domain
Biopharmaceuticals / Nonclinical Safety
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Designing and interpreting in vivo toxicology studies, Regulatory expectations for nonclinical safety datasets, CRO management, In vitro non-GLP study leadership, Cross-functional safety strategy advising, Team mentoring
Preferred skills
PhD in reproductive biology or embryology, Leading GLP study teams, Interpreting in vivo and in vitro data for risk mitigation, Influencing project decisions with data-driven safety recommendations, Working with external partners (CROs, academic collaborators), Matrix team collaboration
Technologies
GLP studies, CRO facilities, In vivo study design, In vitro study design
Responsibilities
Serve as primary contact for reproductive toxicology studies at CROs, Design and oversee reproductive toxicology studies to inform project decisions, Engage external partners to deliver studies on time, Lead internal in vitro non-GLP studies, Advise cross-functional teams on reproductive safety strategy and regulatory needs, Mentor junior scientists
Seniority
Senior, hands-on IC with mentorship responsibilities